<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Dozier C</submitter><funding>Fondation ARC pour la Recherche sur le Cancer</funding><funding>Agence Nationale de la Recherche</funding><pagination>5764</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9144653</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>23(10)</volume><pubmed_abstract>MicroRNAs (miRNAs) are small regulatory non-coding RNAs, resulting from the cleavage of long primary transcripts (pri-miRNAs) in the nucleus by the Microprocessor complex generating precursors (pre-miRNAs) that are then exported to the cytoplasm and processed into mature miRNAs. Some miRNAs are hosted in pri-miRNAs annotated as long non-coding RNAs (lncRNAs) and defined as MIRHGs (for miRNA Host Genes). However, several lnc pri-miRNAs contain translatable small open reading frames (smORFs). If smORFs present within lncRNAs can encode functional small peptides, they can also constitute &lt;i>cis&lt;/i>-regulatory elements involved in lncRNA decay. Here, we investigated the possible involvement of smORFs in the regulation of lnc pri-miRNAs in &lt;i>Human&lt;/i> and &lt;i>Drosophila&lt;/i>, focusing on pri-miR</pubmed_abstract><journal>International journal of molecular sciences</journal><pubmed_title>Small ORFs as New Regulators of Pri-miRNAs and miRNAs Expression in &lt;i>Human&lt;/i> and &lt;i>Drosophila&lt;/i>.</pubmed_title><pmcid>PMC9144653</pmcid><funding_grant_id>ANR biomiPEPs ANR-16-CE12-0018</funding_grant_id><funding_grant_id>ARC PGA1 RF20180206987</funding_grant_id><pubmed_authors>Dozier C</pubmed_authors><pubmed_authors>Montigny A</pubmed_authors><pubmed_authors>Plaza S</pubmed_authors><pubmed_authors>Combier JP</pubmed_authors><pubmed_authors>Viladrich M</pubmed_authors><pubmed_authors>Culerrier R</pubmed_authors><pubmed_authors>Besson A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Small ORFs as New Regulators of Pri-miRNAs and miRNAs Expression in &lt;i>Human&lt;/i> and &lt;i>Drosophila&lt;/i>.</name><description>MicroRNAs (miRNAs) are small regulatory non-coding RNAs, resulting from the cleavage of long primary transcripts (pri-miRNAs) in the nucleus by the Microprocessor complex generating precursors (pre-miRNAs) that are then exported to the cytoplasm and processed into mature miRNAs. Some miRNAs are hosted in pri-miRNAs annotated as long non-coding RNAs (lncRNAs) and defined as MIRHGs (for miRNA Host Genes). However, several lnc pri-miRNAs contain translatable small open reading frames (smORFs). If smORFs present within lncRNAs can encode functional small peptides, they can also constitute &lt;i>cis&lt;/i>-regulatory elements involved in lncRNA decay. Here, we investigated the possible involvement of smORFs in the regulation of lnc pri-miRNAs in &lt;i>Human&lt;/i> and &lt;i>Drosophila&lt;/i>, focusing on pri-miR</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 May</publication><modification>2025-04-22T18:22:13.44Z</modification><creation>2025-04-06T02:23:03.989Z</creation></dates><accession>S-EPMC9144653</accession><cross_references><pubmed>35628573</pubmed><doi>10.3390/ijms23105764</doi></cross_references></HashMap>